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111.
Butyl acrylate, methyl methacrylate, and vinyl acetate solution and emulsion terpolymerizations were conducted. Attenuated total relflection-Fourier transform infrared spectroscopy equipped with conduit and diamond-composite sensor technology was used to monitor solution terpolymerizations off-line and emulsion terpolymerizations in-line. Monomer conversion and terpolymer composition changes as a function of time were calculated by monitoring the peak height of characteristic absorbances of each monomer. Results obtained from the ReactIR™ 1000 reaction-analysis system agreed well with those determined by traditional gravimetry and 1H NMR spectroscopy. For the solution terpolymerizations, improved models developed previously to incorporate solvent effects on solution polymerizations of butyl acrylate and vinyl acetate monomers were applied to predict monomer conversion, copolymer composition, and molecular weight averages. Comparisons between experimental data and model predictions are presented. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1860–1876, 2001 相似文献
112.
醋酸钯催化甲苯中无配体的 Suzuki 反应 总被引:1,自引:0,他引:1
报道了一种甲苯中醋酸钯催化无配体的 Suzuki 反应体系. 以 K3PO4·7H2O 为碱, 在该体系中可高效进行芳基溴代物和芳基硼酸的 Suzuki 反应, 且具有反应条件温和、无需惰性气体保护等特点. 在 n(ArBr) = 0.5 mmol, n(ArB(OH)2) = 0.75 mmol, x(Pd(OAc)2) = 1 mol%, n(K3PO4·7H2O) = 1.0 mmol, v(甲苯) = 2 ml 的优化条件下, 4-溴硝基苯和苯硼酸在 75 °C 反应 5 min, 分离收率即达 99%, TOF 高达 1 188 h?1. 相似文献
113.
Gas phase catalytic oxidation of ethyl acetate and toluene was examined over copper modified ZSM‐5 catalysts under atmospheric pressure. Nanostructure of ZSM‐5 was characterized by XRD, SEM and TEM techniques. Elemental composition of ZSM‐5 was determined using EDX, ICP‐AES and XPS techniques. Results of catalytic studies showed better catalytic activity of Cu‐ZSM‐5 catalysts than those of parent ZSM‐5 and HZSM‐5, which revealed catalytic role of copper ions in the Cu‐ZSM‐5 catalysts. Effects of some parameters over catalytic conversion of these compounds were also studied. Ethyl acetate showed more reactivity than toluene over the Cu‐ZSM‐5 catalysts. Furthermore, the catalytic activity of Cu‐ZSM‐5 catalysts increased with increasing the copper loadings. The conversion behavior of a binary mixture of ethyl acetate and toluene was different from that of a single form. A promotive and inhibitive behavior was observed for conversion of ethyl acetate and toluene in the binary mixture, respectively. Water vapor as co‐feed had an inhibitive effect on conversion of organic compounds over the Cu‐ZSM‐5 catalysts. 相似文献
114.
制备方法对AgCeY吸附剂脱硫性能的影响 《燃料化学学报》2016,44(12):1509-1517
以硅铝比为5.3的NaY分子筛为母体,分别采用微波辅助离子交换法(AgCeY-1)、水热离子交换法(AgCeY-2)和液相离子交换法(AgCeY-3)制备了AgCeY-n吸附剂,并利用XRD、BET、XPS和Py-FTIR对吸附剂进行了表征。以噻吩和苯并噻吩为模型硫化物,甲苯和环己烯为竞争吸附组分,考察了制备方法对制备得到的吸附剂脱硫性能的影响。结果表明,AgCeY-n吸附剂上Ag、Ce元素分别以Ag~+、Ce~(4+)形式存在。经微波辅助离子交换法制备得到的AgCeY-1吸附剂表面Ag~+、Ce~(4+)含量均最高,且具有最高的L酸和B酸量。AgCeY-n吸附剂对硫化物的吸附选择大小顺序为:BTTP,竞争吸附组分对AgCeY-n吸附脱硫性能的影响顺序为:环己烯甲苯。在所研究的制备方法中,微波辅助离子交换法所需时间最短(20 min),合成的AgCeY-1对所研究的模拟油的吸附效果均最好,且具有较好的重复使用性能。各吸附剂对TP和BT的脱除能力大小顺序为:AgCeY-1AgCeY-2AgCeY-3。 相似文献
115.
116.
Ingeborg Csöregh Edwin Webe Thomas Hens 《Journal of inclusion phenomena and macrocyclic chemistry》2000,38(1-4):397-412
Three crystalline inclusion compounds of roof-shapedtrans-11,12-bis(diaryl-hydroxymethyl)-9,10-dihydro-9,10-ethanoanthracene host molecules [where aryl is 4-methyl-phenyl (3) or4-t-butylphenyl (4)] have been studied by X-ray diffraction.The crystals of both the 3methanol (2 : 1) [a = 10.755(1),b = 11.571(1), c = 14.697(2) Å, = 75.12(1), = 89.67(1), = 87.13(1) °] and the 4-pyridine (2 : 3) compounds[a = 14.045(3), b = 14.366(3), c = 15.607(3) Å, = 91.62(1), = 103.65(1) and =116.05(1)°] are triclinic (P–1),while the 3toluene (1 : 1) complex has orthorhombic (Fddd) symmetry [a = 16.041(1), b = 25.008(1), c = 40.440(4) Å]. The host–guest interactions in both triclinic crystals are characterised by hydrogen bonds, with different patterns however. The determined crystal structures indicate a compromise between the requirement of hydrogen bonding on the one hand and close packing on the other. The highly symmetrical host framework in the toluene (1 : 1) complex of 3 seems to be the result of shape recognition, although atendency towards weak (Cmethyl)H arylinteractions [Cmethyl = 3.533(7) and 3.674(6) Å] between the hosts was observed. The present roof-shaped diol hosts give excellent examples of molecular recognition by exhibiting two significantly different conformations, mostly depending on the proton donor/acceptor ability of the guest component. (O)H O intramolecular bonding between the two alcoholic groups characterises the so-called active form, whereas weaker (O)H and interactions stabilise the `inactive'conformation. 相似文献
117.
COPU/PMMA AB交联聚合物的性能 总被引:1,自引:0,他引:1
AB交联聚合物(ABCP)是由聚合物A链与化学组成不同的聚合物B链交联构成。它的网络结构不同于IPN。IPN是由两个独立的网络构成,而在ABCP中仅存在一个聚合物网络。目前人们对它远不及对IPN了解得多。 本文选用蓖麻油为原料,与甲基丙烯酸甲酯共聚,合成了一种ABCP。研究了它的力学性能,转变与松弛,相容性及形态结构与组成及交联密度的关系。 相似文献
118.
在恒温控湿的环境舱中,以自制的TiO2/ACF(活性炭纤维)为光催化剂,研究了环境湿度对甲苯光催化降解过程的影响.通过N2吸附和扫描电子显微镜分别对TiO2/ACF光催化剂的孔径结构和形貌特征进行了表征;利用GC—MS和GC—FID对甲苯光催化过程中生成的中间产物进行了定性及定量分析.结果表明,环境舱中相对湿度增大,甲苯光催化转化率提高;不同相对湿度下,积累在光催化剂表面的中间产物种类相同,但支链氧化产物(苯甲醇、苯甲醛和苯甲酸)的积累量远多于苯环氧化产物(甲酚和对甲基苯酚)的积累量;随环境相对湿度的增大.苯甲醛在光催化剂表面的积累量减小,其余中间产物的积累量均有不同程度的增加.这说明水分子在甲苯光催化过程中起重要作用,相对湿度不仅影响甲苯的光催化转化效率,还影响其光催化转化的过程.尽管在各湿度条件下,支链氧化都是甲苯光催化降解的主要途径,但环境湿度增大更有利于苯环氧化途径的进行.讨论了水蒸气在甲苯光催化氧化过程中的作用机理. 相似文献
119.
应用碰撞诱导解离技术, 研究了甲苯自身化学电离条件下离子-分子反应产物离子m/z 182和184的碰撞诱导解离(CID)反应特性。m/z183和184离子碎裂反应具有多种过渡态结构, 如二苯基甲烷衍生物结构、卓翁离子与甲苯形成的共价键结构、甲苯自由基离子与甲苯分子形成的π-配合物结构和苄基离子与甲苯形成的π-配合物结构。 相似文献
120.
Depolymerization of Poly(bisphenol A carbonate) in Subcritical and Supercritical Toluene 总被引:1,自引:0,他引:1
Zhi Yan PAN Zhen BAO Ying Xu CHEN 《中国化学快报》2006,17(4):545-548
The depolymerization of poly(bisphenol A carbonate)(PC) in subcritical and supercritical toluene was studied. The experimental parameters, which influence the depolymerization reaction such as temperature (570-633 K), pressure (4.0-7.0 MPa), reaction time (5-60 min), and toluene to PC weight ratio (3.0-11.0), were investigated, and the reaction products were determined by GC, GC/MS and FT-IR spectrometer. It was found that the main product of the depolymerization reaction was bisphenol A(BPA). BPA accounted for over 55.7% of the depolymerization products at reaction temperature 613 K, pressure 5.0-6.0 MPa, reaction time 15 min and toluene/PC weight ratio of around 7.0. 相似文献